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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does EBIXA Cause Type i hypersensitivity? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Type i hypersensitivity have been filed in association with EBIXA. This represents 17.9% of all adverse event reports for EBIXA.

5
Reports of Type i hypersensitivity with EBIXA
17.9%
of all EBIXA reports
0
Deaths
5
Hospitalizations

How Dangerous Is Type i hypersensitivity From EBIXA?

Of the 5 reports, 5 (100.0%) required hospitalization.

Is Type i hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EBIXA. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does EBIXA Cause?

Fall (11) Somnolence (8) Convulsion (7) Myoclonus (7) Balance disorder (6) Dyspnoea (6) Gait disturbance (6) Weight increased (6) Delirium (5) Drug prescribing error (5)

What Other Drugs Cause Type i hypersensitivity?

OXALIPLATIN (266) AMOXICILLIN (260) LEVOFLOXACIN (180) ACETAMINOPHEN (129) CARBOPLATIN (125) DICLOFENAC (111) PANTOPRAZOLE (110) PACLITAXEL (107) IBUPROFEN (103) OMEPRAZOLE (98)

Related Pages

EBIXA Full Profile All Type i hypersensitivity Reports All Drugs Causing Type i hypersensitivity EBIXA Demographics